Canonical Allele Identifier: CA452781911

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190122-C-G
• MyVariant Identifiers: chr6:g.157511256C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190122C>G , CM000668.2:g.157190122C>G	GRCh38
NC_000006.11:g.157511256C>G , CM000668.1:g.157511256C>G	GRCh37
NC_000006.10:g.157552948C>G	NCBI36
NG_032093.1:g.417193C>G
NG_032093.2:g.417193C>G
NG_066624.1:g.419097C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3984C>G	ENSP00000055163.8:p.Ala1328=
ENST00000414678.8:c.4053C>G	ENSP00000412835.3:p.Ala1351=
ENST00000637015.2:c.4272C>G	ENSP00000489729.2:p.Ala1424=
ENST00000346085.10:c.4023C>G	ENSP00000344546.5:p.Ala1341=
ENST00000350026.10:c.3735C>G	ENSP00000055163.7:p.Ala1245=
ENST00000414678.7:c.2301C>G	ENSP00000412835.2:p.Ala767=
ENST00000635849.1:c.1464C>G	ENSP00000490948.1:p.Ala488=
ENST00000635957.1:c.1095C>G	ENSP00000490385.1:p.Ala365=
ENST00000636930.2:c.4143C>G MANE Select	ENSP00000490491.2:p.Ala1381=
ENST00000636940.1:n.2140C>G
ENST00000637015.1:c.1511C>G
ENST00000637568.1:c.1425C>G
ENST00000637741.1:n.809C>G
ENST00000637810.1:c.1485C>G	ENSP00000489636.1:p.Ala495=
ENST00000637904.1:c.1644C>G	ENSP00000490550.1:p.Ala548=
ENST00000647938.1:c.3774C>G	ENSP00000498155.1:p.Ala1258=
ENST00000346085.9:c.3774C>G	ENSP00000344546.4:p.Ala1258=
ENST00000350026.9:c.3735C>G	ENSP00000055163.7:p.Ala1245=
ENST00000414678.6:c.2301C>G	ENSP00000412835.2:p.Ala767=
NM_017519.2:c.3735C>G	NP_059989.2:p.Ala1245=
NM_020732.3:c.3774C>G	NP_065783.3:p.Ala1258=
XM_005267069.3:c.3894C>G	XP_005267126.2:p.Ala1298=
XM_011535984.1:c.2973C>G	XP_011534286.1:p.Ala991=
XM_011535985.1:c.2793C>G	XP_011534287.1:p.Ala931=
XM_011535986.1:c.2553C>G	XP_011534288.1:p.Ala851=
XM_011535987.1:c.2172C>G	XP_011534289.1:p.Ala724=
XM_011535988.1:c.1035C>G	XP_011534290.1:p.Ala345=
NM_001346813.1:c.3894C>G	NP_001333742.1:p.Ala1298=
NM_001363725.1:c.1644C>G	NP_001350654.1:p.Ala548=
XM_011535984.2:c.4104C>G	XP_011534286.2:p.Ala1368=
XM_011535988.3:c.1035C>G	XP_011534290.1:p.Ala345=
XM_017011103.2:c.4005C>G	XP_016866592.1:p.Ala1335=
XM_017011104.1:c.3975C>G	XP_016866593.1:p.Ala1325=
XM_017011105.2:c.3945C>G	XP_016866594.1:p.Ala1315=
XM_017011106.2:c.3816C>G	XP_016866595.1:p.Ala1272=
XM_017011107.2:c.3795C>G	XP_016866596.1:p.Ala1265=
XR_002956289.1:n.4187C>G
NM_001363725.2:c.1644C>G	NP_001350654.1:p.Ala548=
NM_001371656.1:c.4023C>G	NP_001358585.1:p.Ala1341=
NM_001374820.1:c.4023C>G	NP_001361749.1:p.Ala1341=
NM_001374828.1:c.4143C>G MANE Select	NP_001361757.1:p.Ala1381=
NM_017519.3:c.3984C>G	NP_059989.3:p.Ala1328=